IRB/RAB

Assurance of Compliance

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    Name Description Status Source
    IRB Registration Valid Through 4.9.2028 Required IRB Registration IORG0000481 through 4.9.2028.pdf Edit IRB Registration Valid Through 4.9.2028 Delete IRB Registration Valid Through 4.9.2028
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While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
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IRB Operating Code and Clinical Research Policy Manual

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    Name Description Status Source
    Clinical Research Policy Manual - IRB Required Clinical Research Policy Manual 2017.pdf Edit Clinical Research Policy Manual - IRB Delete Clinical Research Policy Manual - IRB
    IRB Operating Code Required Institutional Review Board - Operating Code Suggested Edits updated 8.5.2024.pdf Edit IRB Operating Code Delete IRB Operating Code
    While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
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Institutional Review Board (IRB)

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    New Protocol Application Form
    Required
    02 New Protocol Application Form - 2.8.21.docx
    Human Research Protection Education Training PI Investigator
    Required
    03 Human Research Protection Education Training PI.docx
    Research Team Attachment
    Required
    04 Research Team Attachment - Jan 2021.docx
    PI responsibility form
    Required
    05 PI responsibility form - Jan 2021.docx
    IRB - Consent Form Template
    Required
    06 IRB - Consent Form Template - Jan 2021.docx
    Biomedical Research Consent Template
    Required
    06a Biomedical Research Consent Template - Jan 2021.docx
    Biomedical Research Consent Template Additional
    Required
    06b Biomedical Research Consent Template Additional.docx
    Subjects PHI Authorization Form
    Required
    08 Subjects PHI Authorization Form - Jan 2021.docx
    Appendix A - Research Equipment Form
    Required
    13 Appendix A Research Equipment Form - Jan 2021.docx
    Appendix B1 - Device Form
    Required
    09 Appendix B1 Device Form - Jan 2021.docx
    Appendix B2 - Drug and Chemical Usage Form
    Required
    11 Appendix B2 Drug and Chemical Usage Form - Ja.docx
    Appendix C - Biological Materials Form
    Required
    10 Appendix C Biological materials form - Jan 20.docx
    Local Contextual Review
    Required
    12 IRB Local Contextual Review - Jan 2021.docx
    Research Insurance Coverage protocol
    Required
    14 Research Insurance Coverage protocol - Jan 20.doc
    IRB termination form
    Required
    15 IRB termination form.docx
    Required Product Information
    Required
    07 Required Product Information - Jan 2021.docx
    While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
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Informed Consent

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    Name Description Status Source
    Consent Form Template Required 8. IRB - Consent Form Template - Jan 2021.docx Edit Consent Form Template Delete Consent Form Template
    Biomedical Research Consent Template Required 9. Biomedical Research Consent Template - Jan 2021.docx Edit Biomedical Research Consent Template Delete Biomedical Research Consent Template
    Biomedical Research Consent Template Additional Required 10. Biomedical Research Consent Template Additional - Jan 2021.docx Edit Biomedical Research Consent Template Additional Delete Biomedical Research Consent Template Additional
    While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
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Adverse Event/Protocol Deviation

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    Protocol Deviation
    Required
    protocoldeviationform_0.docx
    Adverse Event Report Form
    Required
    Adverse Event Report Form.docx
    Protocol Amendment Form
    Required
    Protocol Amendment Form.docx
    While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
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Start Here

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    Determination Of Human Subject Research

    Does your project require IRB approval?

    Required
    001 Determination Of Human Subject Research.docm
    RAB - Application

    Once you have determined your study needs IRB approval, you will need to go through RAB review first.  Complete and submit form to Dr. Arben Lasku (a.lasku@scnm.edu).

    Required
    01 RAB - Application.docx
    IRB Application Process and Check List
    Required
    2. IRB Application Process and Check List - 2.8.2.docx
    While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
While focused on a reorder icon, press the Enter key or spacebar to "select" the icon. While a reorder icon is selected, pressing the up and down arrows will change the order of the selected item within the list. Pressing Enter key or spacebar again will drop the selected item at that location in the list.
Edit the following settings for all selected Resources.
Select a start and end date and time
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End: End: